scholarly journals Interference with the quorum sensing systems in a Vibrio harveyi strain alters the growth rate of gnotobiotically cultured rotifer Brachionus plicatilis

2007 ◽  
Vol 103 (1) ◽  
pp. 194-203 ◽  
Author(s):  
N.T.N. Tinh ◽  
N.D. Linh ◽  
T.K. Wood ◽  
K. Dierckens ◽  
P. Sorgeloos ◽  
...  
2004 ◽  
Vol 186 (20) ◽  
pp. 6902-6914 ◽  
Author(s):  
Jennifer M. Henke ◽  
Bonnie L. Bassler

ABSTRACT In a process called quorum sensing, bacteria communicate using extracellular signal molecules termed autoinducers. Two parallel quorum-sensing systems have been identified in the marine bacterium Vibrio harveyi. System 1 consists of the LuxM-dependent autoinducer HAI-1 and the HAI-1 sensor, LuxN. System 2 consists of the LuxS-dependent autoinducer AI-2 and the AI-2 detector, LuxPQ. The related bacterium, Vibrio cholerae, a human pathogen, possesses System 2 (LuxS, AI-2, and LuxPQ) but does not have obvious homologues of V. harveyi System 1. Rather, System 1 of V. cholerae is made up of the CqsA-dependent autoinducer CAI-1 and a sensor called CqsS. Using a V. cholerae CAI-1 reporter strain we show that many other marine bacteria, including V. harveyi, produce CAI-1 activity. Genetic analysis of V. harveyi reveals cqsA and cqsS, and phenotypic analysis of V. harveyi cqsA and cqsS mutants shows that these functions comprise a third V. harveyi quorum-sensing system that acts in parallel to Systems 1 and 2. Together these communication systems act as a three-way coincidence detector in the regulation of a variety of genes, including those responsible for bioluminescence, type III secretion, and metalloprotease production.


2013 ◽  
Vol 5 (2) ◽  
pp. 189-193
Author(s):  
A.A. Ortega-Salas ◽  
H. Reyes-Bustamante

The microalgae Chaetoceros gracilis was cultivated to feed the rotifer Brachionus plicatilis. Microalgae and rotifers were grown separately, each for 10 days in a growing system volume of 62,5mL to 20L (1st phase). This was followed by 10 days in 250L (2nd phase), after 10 days in 1 500L (3rd phase). The growth rate exponential population at intervals of 24h for C. gracilis was 0,72, 0,30, and 0,28cells/mL to three phases of cultivation. Within 24h the arithmetic growth rate for the population of B. plicatilis was 330, 1 858 and 13 912rotifers/day in three phases of cultivation. Twenty-four hour intervals counts from the increasing number of organisms in the cultivation of microalgae, allows the prediction of a rotifer production necessary to feed a certain number organisms.KEY WORDSRotifer culture, population growth, fecundity, Chaetoceros culture


2003 ◽  
Vol 185 (3) ◽  
pp. 809-822 ◽  
Author(s):  
Xuesong He ◽  
William Chang ◽  
Deanne L. Pierce ◽  
Laura Ort Seib ◽  
Jennifer Wagner ◽  
...  

ABSTRACT Rhizobium sp. strain NGR234 forms symbiotic, nitrogen-fixing nodules on a wide range of legumes via functions largely encoded by the plasmid pNGR234a. The pNGR234a sequence revealed a region encoding plasmid replication (rep) and conjugal transfer (tra) functions similar to those encoded by the rep and tra genes from the tumor-inducing (Ti) plasmids of Agrobacterium tumefaciens, including homologues of the Ti plasmid quorum-sensing regulators TraI, TraR, and TraM. In A. tumefaciens, TraI, a LuxI-type protein, catalyzes synthesis of the acylated homoserine lactone (acyl-HSL) N-3-oxo-octanoyl-l-homoserine lactone (3-oxo-C8-HSL). TraR binds 3-oxo-C8-HSL and activates expression of Ti plasmid tra and rep genes, increasing conjugation and copy number at high population densities. TraM prevents this activation under noninducing conditions. Although the pNGR234a TraR, TraI, and TraM appear to function similarly to their A. tumefaciens counterparts, the TraR and TraM orthologues are not cross-functional, and the quorum-sensing systems have differences. NGR234 TraI synthesizes an acyl-HSL likely to be 3-oxo-C8-HSL, but traI mutants and a pNGR234a-cured derivative produce low levels of a similar acyl-HSL and another, more hydrophobic signal molecule. TraR activates expression of several pNGR234a tra operons in response to 3-oxo-C8-HSL and is inhibited by TraM. However, one of the pNGR234a tra operons is not activated by TraR, and conjugal efficiency is not affected by TraR and 3-oxo-C8-HSL. The growth rate of NGR234 is significantly decreased by TraR and 3-oxo-C8-HSL through functions encoded elsewhere in the NGR234 genome.


Cell ◽  
2002 ◽  
Vol 110 (3) ◽  
pp. 303-314 ◽  
Author(s):  
Melissa B. Miller ◽  
Karen Skorupski ◽  
Derrick H. Lenz ◽  
Ronald K. Taylor ◽  
Bonnie L. Bassler

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